Nothing Special   »   [go: up one dir, main page]

AU575668B2 - N - acylpyrrolidine compound - Google Patents

N - acylpyrrolidine compound

Info

Publication number
AU575668B2
AU575668B2 AU45597/85A AU4559785A AU575668B2 AU 575668 B2 AU575668 B2 AU 575668B2 AU 45597/85 A AU45597/85 A AU 45597/85A AU 4559785 A AU4559785 A AU 4559785A AU 575668 B2 AU575668 B2 AU 575668B2
Authority
AU
Australia
Prior art keywords
compound
acylpyrrolidine
prolyl endopeptidase
active ingredient
well
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
AU45597/85A
Other versions
AU4559785A (en
Inventor
Masaki Hashimoto
Naoki Higuchi
Masayuki Saito
Takaharu Tanaka
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Suntory Ltd
Original Assignee
Suntory Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Suntory Ltd filed Critical Suntory Ltd
Publication of AU4559785A publication Critical patent/AU4559785A/en
Application granted granted Critical
Publication of AU575668B2 publication Critical patent/AU575668B2/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

A novel compound that exhibits inhibitory activity against prolyl endopeptidase and a method for chemical synthesis of said compound, as well as its use as a prolyl endopeptidase inhibitor and an anti-amnesic agent that contains said compound as the active ingredient are provided.
AU45597/85A 1984-07-31 1985-07-30 N - acylpyrrolidine compound Ceased AU575668B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP59-160994 1984-07-31
JP16099484A JPS6137764A (en) 1984-07-31 1984-07-31 Novel physiologically active compound having anti-prolyl-endopeptidase activity

Publications (2)

Publication Number Publication Date
AU4559785A AU4559785A (en) 1986-02-06
AU575668B2 true AU575668B2 (en) 1988-08-04

Family

ID=15726550

Family Applications (1)

Application Number Title Priority Date Filing Date
AU45597/85A Ceased AU575668B2 (en) 1984-07-31 1985-07-30 N - acylpyrrolidine compound

Country Status (6)

Country Link
US (1) US4743616A (en)
EP (1) EP0172458B1 (en)
JP (1) JPS6137764A (en)
AT (1) ATE47711T1 (en)
AU (1) AU575668B2 (en)
DE (1) DE3574014D1 (en)

Families Citing this family (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4873342A (en) * 1985-04-16 1989-10-10 Suntory Limited Dipeptide derivative and synthesis and use thereof
JPH0623190B2 (en) * 1985-04-16 1994-03-30 サントリー株式会社 N-acylpyrrolidine derivative having inhibitor activity, process for producing the same and use thereof
CA1320734C (en) * 1986-02-04 1993-07-27 Suntory Limited Pyrrolidineamide derivative of acylamino acid and pharmaceutical composition containing the same
US5198458A (en) * 1986-02-04 1993-03-30 Suntory Limited Pyrrolidineamide derivatives of acylamino acid and pharmaceutical composition containing the same
US4880827A (en) * 1986-03-18 1989-11-14 Sumitomo Pharmaceuticals Company, Ltd. Pyrrolidine derivatives having inhibitory action for proline specific endopepidase
JPH08806B2 (en) * 1986-11-18 1996-01-10 サントリー株式会社 Novel pyrrolidine amide derivative having prolyl endopeptidase inhibitory action
DE3786229T2 (en) * 1986-11-20 1993-10-07 Ono Pharmaceutical Co Prolinal derivatives.
US5254550A (en) * 1986-11-20 1993-10-19 Ono Pharmaceutical Co., Ltd. Prolinal derivatives and pharmaceutical compositions thereof
ES2046195T3 (en) * 1986-12-29 1994-02-01 Ono Pharmaceutical Co., Ltd. A PROCEDURE FOR THE PREPARATION OF PROLINAL DERIVATIVES.
US5262431A (en) * 1986-12-29 1993-11-16 Ono Pharmaceutical Co., Ltd. Prolinal derivatives and pharmaceutical compositions thereof
ATE87306T1 (en) * 1987-02-04 1993-04-15 Ono Pharmaceutical Co PROLINAL DERIVATIVES.
EP0280956B1 (en) * 1987-02-23 1992-10-21 Ono Pharmaceutical Co., Ltd. Thiazolidine derivatives
DE3712365A1 (en) * 1987-04-11 1988-10-27 Hoechst Ag NEW 2-ACYLPYRROLIDINE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF, CONTAINERS AND THE USE THEREOF
DE3712364A1 (en) * 1987-04-11 1988-10-27 Hoechst Ag NEW PYRROLIDIN-2 (1,3-DICARBONYL) DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF, THE CONTAINERS AND THE USE THEREOF
JPH0774194B2 (en) * 1987-06-11 1995-08-09 財団法人微生物化学研究会 A novel actinonine derivative with physiological activity
JP2691442B2 (en) * 1989-02-20 1997-12-17 株式会社ヤクルト本社 Novel proline derivative
WO1990012005A1 (en) * 1989-04-13 1990-10-18 Japan Tobacco Inc. New amino acid derivatives having prolylendopeptidase inhibitor activity
US5073549A (en) * 1990-03-22 1991-12-17 Bristol-Myers Squibb Company BU-4164E - A and B, prolyl endopeptidase inhibitors and their methods of use
US4999349A (en) * 1990-03-22 1991-03-12 Bristol-Myers Squibb Co. BU-4164E - A and B, prolyl endopeptidase inhibitors
FR2669029B1 (en) * 1990-11-14 1994-09-02 Adir NOVEL N-BENZOYL PROLINE DERIVATIVES, THEIR PREPARATION PROCESS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM.
US5620971A (en) * 1991-05-09 1997-04-15 Vertex Pharmaceuticals Incorporated Biologically active acylated amino acid derivatives
ATE183178T1 (en) * 1991-05-09 1999-08-15 Vertex Pharma NEW IMMUNOSUPRESSIVE COMPOUNDS
US5723459A (en) * 1991-05-09 1998-03-03 Vertex Pharmaceuticals Incorporated Biologically active acylated amino acid derivatives
MX9202466A (en) * 1991-05-24 1994-06-30 Vertex Pharma NOVELTY IMMUNOSUPPRESSIVE COMPOUNDS.
US5439930A (en) * 1992-04-14 1995-08-08 Russian-American Institute For New Drug Development Biologically active n-acylprolydipeptides having antiamnestic, antihypoxic and anorexigenic effects
US5543423A (en) * 1994-11-16 1996-08-06 Vertex Pharmaceuticals, Incorporated Amino acid derivatives with improved multi-drug resistance activity
TW492957B (en) * 1996-11-07 2002-07-01 Novartis Ag N-substituted 2-cyanopyrrolidnes
JP2003535034A (en) * 1999-11-12 2003-11-25 ギルフォード ファーマシューティカルズ インコーポレイテッド Dipeptidyl peptidase IV inhibitors and methods for producing and using dipeptidyl peptidase IV inhibitors
DE602004026289D1 (en) 2003-05-05 2010-05-12 Probiodrug Ag Glutaminyl INHIBITORS
EP1824846A2 (en) 2003-11-03 2007-08-29 Probiodrug AG Novel compounds for the treatment of neurological disorders
JP2007509898A (en) 2003-11-03 2007-04-19 プロビオドルグ エージー Useful combinations for the treatment of neurological disorders
KR101099206B1 (en) 2004-02-05 2011-12-27 프로비오드룩 아게 Novel Inhibitors of Glutaminyl Cyclase
US20080234344A1 (en) * 2004-03-26 2008-09-25 Jochen Klock Amino Acid and Peptide Conjugates of Arylalkylic Acids for Cosmetic Use
EP2089383B1 (en) 2006-11-09 2015-09-16 Probiodrug AG 3-hydr0xy-1,5-dihydr0-pyrr0l-2-one derivatives as inhibitors of glutaminyl cyclase for the treatment of ulcer, cancer and other diseases
SI2091948T1 (en) 2006-11-30 2012-07-31 Probiodrug Ag Novel inhibitors of glutaminyl cyclase
NZ579310A (en) 2007-03-01 2012-03-30 Probiodrug Ag Use of glutaminyl cyclase inhibitors for the treatment of mild cognitive impairment and diagnostic purposes thereof
EP2142514B1 (en) 2007-04-18 2014-12-24 Probiodrug AG Thiourea derivatives as glutaminyl cyclase inhibitors
WO2009007415A2 (en) * 2007-07-10 2009-01-15 Probiodrug Ag Novel compounds
JP5934645B2 (en) 2009-09-11 2016-06-15 プロビオドルグ エージー Heterocyclic derivatives as glutaminyl cyclase inhibitors
JP6026284B2 (en) 2010-03-03 2016-11-16 プロビオドルグ エージー Inhibitors of glutaminyl cyclase
EA022420B1 (en) 2010-03-10 2015-12-30 Пробиодруг Аг Heterocyclic inhibitors of glutaminyl cyclase (qc, ec 2.3.2.5)
WO2011131748A2 (en) 2010-04-21 2011-10-27 Probiodrug Ag Novel inhibitors
US8530670B2 (en) 2011-03-16 2013-09-10 Probiodrug Ag Inhibitors
PL3461819T3 (en) 2017-09-29 2020-11-30 Probiodrug Ag Inhibitors of glutaminyl cyclase

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4052511A (en) * 1976-02-13 1977-10-04 E. R. Squibb & Sons, Inc. Carboxyacylproline derivatives
US4154937A (en) * 1977-02-11 1979-05-15 E. R. Squibb & Sons, Inc. Hydroxycarbamoylalkylacylpipecolic acid compounds
US4226775A (en) * 1979-06-01 1980-10-07 American Cyanamid Company Substituted thio-substituted benzyl-propionyl-L-prolines
ZA802552B (en) * 1979-05-21 1981-04-29 Ici Ltd 1-phenyl-2-aminoethanol derivatives
US4374847A (en) * 1980-10-27 1983-02-22 Ciba-Geigy Corporation 1-Carboxyalkanoylindoline-2-carboxylic acids
US4479963A (en) * 1981-02-17 1984-10-30 Ciba-Geigy Corporation 1-Carboxyalkanoylindoline-2-carboxylic acids
US4439611A (en) * 1982-06-28 1984-03-27 American Cyanamid Company Isolation of [S-(R*, S*]-1-(3-acetylthio-3-benzoyl-2-methylpropionyl)-L-proline from a diastereomeric mixture

Also Published As

Publication number Publication date
EP0172458A2 (en) 1986-02-26
ATE47711T1 (en) 1989-11-15
EP0172458B1 (en) 1989-11-02
JPH0479334B2 (en) 1992-12-15
AU4559785A (en) 1986-02-06
US4743616A (en) 1988-05-10
JPS6137764A (en) 1986-02-22
EP0172458A3 (en) 1987-01-07
DE3574014D1 (en) 1989-12-07

Similar Documents

Publication Publication Date Title
AU575668B2 (en) N - acylpyrrolidine compound
EP0201742A3 (en) N-acylpyrrolidine derivatives, processes for preparing them, pharmaceutical composition and use
MY111370A (en) Dual action inhibitors
EP0815856A3 (en) Retroviral protease inhibitors
MY106606A (en) Cycloalkyl-substituted glutaramide antihypertensive agents.
NO942064L (en) inhibitors
CA2081970A1 (en) Hiv protease inhibitors useful for the treatment of aids
EP0677048A1 (en) Cyclic sulfone containing retroviral protease inhibitors.
MX9601360A (en) Synergistic stabilizing mixture.
IE810474L (en) Anti-hypertensive agents
AU2733997A (en) N-(amidinophenyl)-n'-(subst.)-3h-2,4-benzodiazepin-3-one derivatives as factor xa inhibitors
GR3024181T3 (en) N-(alkanoylamino-2-hydroxypropyl)-sulfonamides useful as retroviral protease inhibitors.
PL309282A1 (en) Application of 2-amino-6-n-propyl-amino- 4,5,6,7-tetrahydrobenzothiasole (pramipexol) as an antidepressant
TW223630B (en) Retroviral protease inhibitors
AU8350698A (en) Metalloproteinase inhibitors
TWI256892B (en) Plasminogen activator inhibitor and external preparation for skin comprising the same
WO1993009791A3 (en) Use of amphotericin b derivatives as protease inhibitors
ES8205126A1 (en) Angiotensin converting enzyme inhibitors.
AU1235288A (en) Antidepressant compositions
EP0114389A3 (en) Substituted arylglyoxal derivatives
ES2065843A1 (en) Application of manoyl ent-11[beta],16-dihydroxy-18-nor- 4[alpha]-carboxymethyl-oxide as adenylatocyclase inhibitor
ES2065844A1 (en) Application of manoyl ent-16,18-dihydroxy-6-oxo-oxide as adenylatocyclase inhibitor
UA11675A1 (en) 1-beta-oxyethylamino-3-keto-5,5-dimethylcyclohexene-1 having analgetic activity